The Effects of Glucagon on Renal Regional Blood Flow in Humans Measured by Magnetic Resonance.
1 other identifier
interventional
10
0 countries
N/A
Brief Summary
This study will investigating the effects of glucagon on renal blood flow in humans using MRI technology. Glucagon, a hormone produced by the pancreas, plays a key role in regulating blood sugar levels. It has been shown to affect renal function, including electrolyte balance and blood flow, especially in conditions like type 2 diabetes where abnormal glucagon levels are common. The study aims to understand how glucagon affects regional blood flow in the kidneys, specifically the cortex and medulla, and whether these effects are mediated by glucagon receptors. The study will be conducted on 10 healthy male participants aged 20-60 years. It involves three test days where participants will receive either glucagon, glucagon with a GLP-1 receptor antagonist, or placebo. Blood flow, glomerular filtration rate, and other renal functions will be measured using MRI. The study seeks to clarify whether glucagon's effects on the kidneys are linked to changes in regional blood flow and to determine if these effects are mediated solely by glucagon receptors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 21, 2025
CompletedFirst Posted
Study publicly available on registry
March 12, 2025
CompletedStudy Start
First participant enrolled
June 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2027
Study Completion
Last participant's last visit for all outcomes
November 1, 2027
October 3, 2025
September 1, 2025
1.4 years
February 21, 2025
September 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Blood perfusion of the kidney
we would like to measure blood perfusion of the kidneys over time
7 measurements of 10 minutes each from the start of infusion (time 0) and up to one hour (time 60).
Secondary Outcomes (2)
Blood flow of the renal arteries
7 measurements of 10 minutes each from the start of infusion (time 0) and up to one hour (time 60).
blood oxygen saturation of the kidneys
7 measurements of 10 minutes each from the start of infusion (time 0) and up to one hour (time 60).
Study Arms (3)
Glucagon
EXPERIMENTALGlucagon+Exendin9-39
EXPERIMENTALSodium chloride (Placebo comparator)
PLACEBO COMPARATORInterventions
Glucagon infusion at 5 ng·kg-¹·min-¹ from 0-30 minutes and 10 ng·kg-¹·min-¹ from 30-60 minutes.
Glucagon infusion at 5 ng·kg-¹·min-¹ from 0-30 minutes and 10 ng·kg-¹·min-¹ from 30-60 minutes, plus a GLP-1R antagonist, exendin 9-39 (900 pmol·kg-¹·min-¹), given intravenously from -30 to 60 minutes
Placebo (0.9% NaCl).
Eligibility Criteria
You may qualify if:
- Normal health confirmed through; Interview and Medical examination
- Normal values with respect to blood concentrations of fasting plasma glucose, fasting plasma total cholesterol, fasting triglycerides, HDL, LDL, creatinine, liver function tests, and electrolytes
- Informed consent
You may not qualify if:
- Immunosuppressive treatment in the previous 12 months
- Alcohol abuse
- Medical treatment with oral glucocorticoids, dipeptidyl peptidase-4 (DPP-4) inhibitors, or GLP-1 receptor agonists, which, in the opinion of the principal investigator, may interfere with glucose metabolism
- Use of lithium
- Medical treatment that affects insulin secretion or the renin-angiotensin-aldosterone system
- Liver disease (ALT \> 2x normal value)
- Renal impairment (serum creatinine \> 130 µM and/or albuminuria)
- Individuals with severe claustrophobia
- Individuals with MR-incompatible foreign bodies
- Individuals with hypertension
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief Physician, Associate Professor, PhD, MD
Study Record Dates
First Submitted
February 21, 2025
First Posted
March 12, 2025
Study Start (Estimated)
June 1, 2026
Primary Completion (Estimated)
November 1, 2027
Study Completion (Estimated)
November 1, 2027
Last Updated
October 3, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share